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2. [Distribution of skeletal muscle involvement in autosomal recessive distal muscular dystrophy: a clinical and computed tomographic study]. Mizusawa H; Kobayashi F; Nakanishi T Rinsho Shinkeigaku; 1987 Feb; 27(2):177-84. PubMed ID: 3581592 [No Abstract] [Full Text] [Related]
3. [A case of distal muscular dystrophy (Miyoshi), characterized by early involvement in paravertebral muscle and atypical changes in muscle biopsy specimen]. Kamakura K; Shimomura S; Higuchi I; Takatani O Rinsho Shinkeigaku; 1988 Jun; 28(6):665-9. PubMed ID: 3233839 [No Abstract] [Full Text] [Related]
4. [Two sisters with autosomal recessive muscular dystrophy (Miyoshi) with early involvement of limb girdle muscles]. Nishida Y; Ishimoto S; Kobayashi T; Goto I; Kuroiwa Y; Mitsuo K; Higashi Y Rinsho Shinkeigaku; 1987 Jun; 27(6):756-9. PubMed ID: 3665270 [No Abstract] [Full Text] [Related]
5. Computed tomography of muscle. Bulcke JA; Crolla D; Termote JL; Baert A; Palmers Y; Van den Bergh R Muscle Nerve; 1981; 4(1):67-72. PubMed ID: 7231448 [TBL] [Abstract][Full Text] [Related]
6. Early onset muscular dystrophy with autosomal dominant heredity. Report of a family and CT findings of skeletal muscle. Tohyama J; Inagaki M; Nonaka I Brain Dev; 1994; 16(5):402-6. PubMed ID: 7892962 [TBL] [Abstract][Full Text] [Related]
7. Distal anterior compartment myopathy: a dysferlin mutation causing a new muscular dystrophy phenotype. Illa I; Serrano-Munuera C; Gallardo E; Lasa A; Rojas-García R; Palmer J; Gallano P; Baiget M; Matsuda C; Brown RH Ann Neurol; 2001 Jan; 49(1):130-4. PubMed ID: 11198284 [TBL] [Abstract][Full Text] [Related]
8. Autosomal recessive distal muscular dystrophy: a comparative study with distal myopathy with rimmed vacuole formation. Nonaka I; Sunohara N; Satoyoshi E; Terasawa K; Yonemoto K Ann Neurol; 1985 Jan; 17(1):51-9. PubMed ID: 3985587 [TBL] [Abstract][Full Text] [Related]
9. Muscle fiber immaturity and inactivity reduce myonecrosis in Duchenne muscular dystrophy. Kimura S; Sugino S; Ohtani Y; Matsukura M; Nishino I; Ikezawa M; Sakata A; Kondo Y; Yoshioka K; Huard J; Nonaka I; Miike T Ann Neurol; 1998 Dec; 44(6):967-71. PubMed ID: 9851444 [TBL] [Abstract][Full Text] [Related]
10. Computerized tomography and magnetic resonance muscle imaging in Miyoshi's myopathy. Meola G; Sansone V; Rotondo G; Jabbour A Muscle Nerve; 1996 Nov; 19(11):1476-80. PubMed ID: 8874406 [TBL] [Abstract][Full Text] [Related]
11. Computed tomographic findings in manifesting carriers of Duchenne muscular dystrophy. de Visser M; Verbeeten B Clin Genet; 1985 Mar; 27(3):269-75. PubMed ID: 3987077 [TBL] [Abstract][Full Text] [Related]
12. [Quantitative computed tomographic studies of disseminated muscle changes in female carriers of Becker-Kiener muscular dystrophy]. Huppert P; Spiegler AW Radiol Diagn (Berl); 1987; 28(2):205-16. PubMed ID: 3615835 [No Abstract] [Full Text] [Related]
15. Distal muscular dystrophy of Miyoshi type. Report of two cases and review of the literature. Flachenecker P; Kiefer R; Naumann M; Handwerker M; Reichmann H J Neurol; 1997 Jan; 244(1):23-9. PubMed ID: 9007741 [TBL] [Abstract][Full Text] [Related]
16. [Cranial X-ray CT and MRI in congenital muscular dystrophy]. Horikawa H; Konishi T; Konagaya M; Mano Y; Takayanagi T Rinsho Shinkeigaku; 1988 Jan; 28(1):102-6. PubMed ID: 3383509 [No Abstract] [Full Text] [Related]
17. [A single case of autosomal recessive muscular dystrophy of childhood--histological and immunocytochemical studies on biopsied muscle]. Tachi N; Sasaki K; Yamada T No To Hattatsu; 1990 Sep; 22(5):514-6. PubMed ID: 2223192 [No Abstract] [Full Text] [Related]
18. [The usefulness of computed tomography in studying Becker's muscular dystrophy. Apropos of a case]. Campanile S; Cerisoli M; Amore M; Campanile A Radiol Med; 1989 Apr; 77(4):418-9. PubMed ID: 2727347 [No Abstract] [Full Text] [Related]
19. Late-onset autosomal recessive limb-girdle muscular dystrophy with rimmed vacuoles. Nakamura A; Yoshida K; Ikeda S Clin Neurol Neurosurg; 2004 Mar; 106(2):122-8. PubMed ID: 15003303 [TBL] [Abstract][Full Text] [Related]
20. An autosomal dominant type of congenital muscular dystrophy. Leyten QH; Gabreëls FJ; Joosten EM; Renier WO; Ter Laak HJ; Ter Haar BG; Stadhouders AM Brain Dev; 1986; 8(5):533-7. PubMed ID: 3799922 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]